Variant #0000860084 (NC_000006.11:g.116446633A>C, NM_000493.3:c.23T>G (COL10A1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.116446633A>C
DNA change (hg38) -
Published as COL10A1(NM_000493.3):c.23T>G (p.(Leu8Trp))
ISCN -
DB-ID COL10A1_000019
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00089 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL10A1 NM_000493.3 -?/. - c.23T>G r.(?) p.(Leu8Trp)
NT5DC1 NM_152729.2 -?/. - c.529+7525A>C r.(=) p.(=)


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